ArticleJournal of research in medical sciences : the official journal of Isfahan University of Medical Sciences2019
Molecular genetic analysis of polycystic kidney disease 1 and polycystic kidney disease 2 mutations in pedigrees with autosomal dominant polycystic kidney disease.
Article in Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.
What it found
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The trial behind it
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Who cites it
4 citing papers in PubMed, 1 synthesis or guideline pooled it, 6 citations in OpenAlex.
- NOS3 gene intron 4 a/b polymorphism is associated with ESRD in autosomal dominant polycystic kidney disease patients.Jornal brasileiro de nefrologiaPooled it
- Targeted Next Generation Sequencing Revealed Novel Variants in theArchives of Iranian medicine · 2022Article
- Pericardial Effusion on MRI in Autosomal Dominant Polycystic Kidney Disease.Journal of clinical medicine · 2022Article
- Molecular Diagnostics of Ciliopathies and Insights Into Novel Developments in Diagnosing Rare Diseases.British journal of biomedical science · 2022Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundDysfunction of polycystin-1 or polycystin-2, the proteins encoded by polycystic kidney disease 1 ( MATERIALS AND
methodsIn this study, mutation analysis of
resultsMutations were found in all 9 families in
conclusionFinding more mutations and expanding the spectrum of
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.